Stereotactic ablative body radiotherapy with a central high dose using CyberKnife for metastatic lung tumors.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
07 Mar 2023
Historique:
received: 13 12 2022
accepted: 13 02 2023
entrez: 7 3 2023
pubmed: 8 3 2023
medline: 10 3 2023
Statut: epublish

Résumé

The CyberKnife system features a robotically-positioned linear accelerator to deliver real-time image-guided stereotactic ablative body radiotherapy (SABR). It achieves steep dose gradients using irradiation from hundreds of different directions and increases the central dose of the gross tumor volume (GTV) without increasing the marginal dose to the planning target volume. We evaluated the effectiveness and safety of SABR with a central high dose using CyberKnife for metastatic lung tumors. A total of 73 patients with 112 metastatic lung tumors treated with CyberKnife were retrospectively analyzed. Local control, progression-free survival, and overall survival were calculated using the Kaplan-Meier method. The median age was 69.2 years. The most common primary sites were the uterus (n = 34), colorectum (n = 24), head and neck (n = 17), and esophagus (n = 16). For peripheral lung tumors, the median radiation dose was 52 Gy in 4 fractions, whereas for centrally located lung tumors, it was 60 Gy in 8-10 fractions. The dose prescription was defined as 99% of the solid tumor components of the GTV. The median maximum dose within the GTV was 61.0 Gy. The GTV and planning target volume were enclosed conformally by the 80% and 70% isodose lines of the maximum dose, respectively. The median follow-up period was extended to 24.7 months; it was 33.0 months for survivors. The 2-year local control, progression-free survival, and overall survival rates were 89.1%, 37.1%, and 71.3%, respectively. Toxicities of grade ≥ 2 were noted as grade 2 and 3 radiation pneumonitis in one patient each. The two patients with grade 2 or higher radiation pneumonitis had both received simultaneous irradiation at two or three metastatic lung tumor sites. No toxicity of grade ≥ 2 was observed in patients with metastasis in one lung only. SABR with a central high dose using CyberKnife for metastatic lung tumors is effective with acceptable toxicity. Number: 20557, Name: Stereotactic ablative radiotherapy using CyberKnife for metastatic lung tumor, URL: http://www.radonc.med.osaka-u.ac.jp/pdf/SBRT.pdf , Date of registration: April 1, 2021 (retrospectively registered), Date of enrollment: May 1, 2014.

Sections du résumé

BACKGROUND BACKGROUND
The CyberKnife system features a robotically-positioned linear accelerator to deliver real-time image-guided stereotactic ablative body radiotherapy (SABR). It achieves steep dose gradients using irradiation from hundreds of different directions and increases the central dose of the gross tumor volume (GTV) without increasing the marginal dose to the planning target volume. We evaluated the effectiveness and safety of SABR with a central high dose using CyberKnife for metastatic lung tumors.
METHODS METHODS
A total of 73 patients with 112 metastatic lung tumors treated with CyberKnife were retrospectively analyzed. Local control, progression-free survival, and overall survival were calculated using the Kaplan-Meier method. The median age was 69.2 years. The most common primary sites were the uterus (n = 34), colorectum (n = 24), head and neck (n = 17), and esophagus (n = 16). For peripheral lung tumors, the median radiation dose was 52 Gy in 4 fractions, whereas for centrally located lung tumors, it was 60 Gy in 8-10 fractions. The dose prescription was defined as 99% of the solid tumor components of the GTV. The median maximum dose within the GTV was 61.0 Gy. The GTV and planning target volume were enclosed conformally by the 80% and 70% isodose lines of the maximum dose, respectively. The median follow-up period was extended to 24.7 months; it was 33.0 months for survivors.
RESULTS RESULTS
The 2-year local control, progression-free survival, and overall survival rates were 89.1%, 37.1%, and 71.3%, respectively. Toxicities of grade ≥ 2 were noted as grade 2 and 3 radiation pneumonitis in one patient each. The two patients with grade 2 or higher radiation pneumonitis had both received simultaneous irradiation at two or three metastatic lung tumor sites. No toxicity of grade ≥ 2 was observed in patients with metastasis in one lung only.
CONCLUSIONS CONCLUSIONS
SABR with a central high dose using CyberKnife for metastatic lung tumors is effective with acceptable toxicity.
TRIAL REGISTRATION BACKGROUND
Number: 20557, Name: Stereotactic ablative radiotherapy using CyberKnife for metastatic lung tumor, URL: http://www.radonc.med.osaka-u.ac.jp/pdf/SBRT.pdf , Date of registration: April 1, 2021 (retrospectively registered), Date of enrollment: May 1, 2014.

Identifiants

pubmed: 36882702
doi: 10.1186/s12885-023-10635-6
pii: 10.1186/s12885-023-10635-6
pmc: PMC9990197
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

215

Subventions

Organisme : Japan Society for the Promotion of Science
ID : JP 20K167250

Informations de copyright

© 2023. The Author(s).

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Auteurs

Kazuhiko Hayashi (K)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan. hayashi@radonc.med.osaka-u.ac.jp.

Osamu Suzuki (O)

Osaka Heavy Ion Therapy Center, Osaka, Japan.

Hiroya Shiomi (H)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Hitoshi Ono (H)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Akira Setoguchi (A)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Masataka Nakai (M)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Erina Nakanishi (E)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Shotaro Tatekawa (S)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Naoko Ose (N)

Department of General Thoracic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.

Takero Hirata (T)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Keisuke Tamari (K)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Yuji Seo (Y)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Soichiro Funaki (S)

Department of General Thoracic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.

Fumiaki Isohashi (F)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Shinichi Shimizu (S)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

Yasushi Shintani (Y)

Department of General Thoracic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.

Kazuhiko Ogawa (K)

Department of Radiation Oncology, Osaka University Graduate School of Medicine, 2-2 (D10) Yamada-Oka, Suita, Osaka, Japan.

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Classifications MeSH